Figure 2
Figure 2. IP administration of Δ12-PGJ3 eradicates FV-leukemia in mice. (A) Spleen weights of FV-infected mice treated with various doses of Δ12-PGJ3 (mg/kg body weight). n = 10 per treatment group. Δ12-PGJ3 treatment at the indicated dosage was started at 1 week after infection for a period of 7 days. *P < .05. Inset: representative spleens from each treatment group. UI indicates uninfected mice. (B) Analysis of LSCs (M34+Kit+Sca1+) in the spleens of FV-infected mice treated with Δ12-PGJ3 or vehicle (Veh) control. (C) FV-CFU formation in Δ12-PGJ3– and vehicle control–treated mice. *P < .001. (D) H&E staining of spleen sections from uninfected (left), FV-infected–vehicle treated (middle), and FV-infected– Δ12-PGJ3–treated mice (right) on day 14 after infection. Small box indicated on each section on the left is magnified on the right side. Scale bars indicate 500 μm.

IP administration of Δ12-PGJ3 eradicates FV-leukemia in mice. (A) Spleen weights of FV-infected mice treated with various doses of Δ12-PGJ3 (mg/kg body weight). n = 10 per treatment group. Δ12-PGJ3 treatment at the indicated dosage was started at 1 week after infection for a period of 7 days. *P < .05. Inset: representative spleens from each treatment group. UI indicates uninfected mice. (B) Analysis of LSCs (M34+Kit+Sca1+) in the spleens of FV-infected mice treated with Δ12-PGJ3 or vehicle (Veh) control. (C) FV-CFU formation in Δ12-PGJ3– and vehicle control–treated mice. *P < .001. (D) H&E staining of spleen sections from uninfected (left), FV-infected–vehicle treated (middle), and FV-infected– Δ12-PGJ3–treated mice (right) on day 14 after infection. Small box indicated on each section on the left is magnified on the right side. Scale bars indicate 500 μm.

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